The Role:

You will be responsible for :

• Providing support for executing industrial trials.
• Coordinating with the business and as well as onsite staff, industrial research coordinators, principal investigators, and vendors to ensure clinical studies meet or exceed timelines and maintain high quality standards.
• Reviewing and monitoring overall industrial data quality and identifying and resolving potential study or site issues.
• Implementing study-specific industrial monitoring tools and documents.
• Ensuring that all trial protocols are followed accurately.

Ideal Profile:

• You have at least 1 year experience including solid experience in a similar role within Healthcare & Lifesciences.
• You are adaptable and thrive in changing environments
• You enjoy finding creative solutions to problems
• You pay strong attention to detail and deliver work that is of a high standard

What's on Offer?

• Attractive Salary & Benefits
• Leadership Role
• Opportunity to make a positive impact